NA 1011-76-000Recalls & reported problems
Depuy Orthopaedics, Inc. · PROTRUSIO CAGE CEMENTED ACETABULAR RECONSTRUCTION 60mm OD 57mm ID LEFT · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295000587), received between Feb 26, 2020 and Feb 26, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Osseointegration Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Osseointegration Problem1
- Unintended Movement1
Patient problems
- Hemorrhage/Blood Loss/Bleeding1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 26, 2020Osseointegration Problem; Unintended Movement; Osseointegration Problem; Unintended Movement
PPF AND STICKER SHEETS RECEIVED. THERE WERE NO ALLEGATIONS REPORTED HOWEVER THE PATIENT WAS REVISED AND THE REASON FOR REVISION WAS NOT PROVIDED. DOI: (B)(6) 2017. DOR: (B)(6) 2018, (LEFT HIP, FIFTH REVISION).
Patient problems: Hemorrhage/Blood Loss/Bleeding; No Code Available
MAUDE report 9753106 ↗
Other Mesh, surgical, acetabular, hip, prosthesis devices
- NA 1011-40-030Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis13 reports
- NA 1011-40-025Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis13 reports
- NA 1011-40-020Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis11 reports
- NA 1011-40-040Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis11 reports
- NA 1011-40-035Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis9 reports
- NA 1011-40-015Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis8 reports
- NA 1011-71-000Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis4 reports
- NA 1011-02-501Depuy Orthopaedics, Inc. · Mesh, surgical, acetabular, hip, prosthesis3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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